Evidence map›Paper›PMID 42645045›Full record

ReviewBiosensors2026

Progress in Optical Methods for the Detection of Two Core Blood Biomarkers of Alzheimer's Disease: Amyloid-Beta and Tau Proteins.

Ning Xia, Fengli Gao, Chuye Zheng

Abstract readReview
In one paragraph

Review in Biosensors, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Ning XiaHenan Province of Key Laboratory of New Optoelectronic Functional Materials, College of Chemistry and Chemical Engineering, Anyang Normal University, Anyang 455000, China.ORCID 0000-0003-0366-7524
Fengli GaoHenan Province of Key Laboratory of New Optoelectronic Functional Materials, College of Chemistry and Chemical Engineering, Anyang Normal University, Anyang 455000, China.
Chuye ZhengHenan Province of Key Laboratory of New Optoelectronic Functional Materials, College of Chemistry and Chemical Engineering, Anyang Normal University, Anyang 455000, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alzheimer's disease (AD) is the most common neurodegenerative disorder worldwide. Early diagnosis of AD is crucial for delaying disease progression and improving patients' quality of life. Blood biomarkers, particularly amyloid-beta (Aβ) and Tau proteins along with their phosphorylated isoforms, show advantages such as convenient sampling, minimal invasiveness, and excellent repeatability. However, the extremely low concentrations of AD biomarkers in blood impose stringent requirements on the sensitivity, specificity, and anti-interference capability of detection methods. Optical methods provide promising analytical platforms to address these challenges in view of their intrinsic merits of high sensitivity and selectivity; rapid response; and potential for miniaturization. This review systematically summarizes the latest advances in optical methods for the detection of the two core AD blood biomarkers (Aβ and Tau), covering techniques such as colorimetry, fluorescence, chemiluminescence, surface plasmon resonance (SPR), and surface-enhanced Raman scattering (SERS). The sensing principles, design strategies, and analytical performances of these methods are discussed, with special emphasis on different signal amplification strategies. In addition, several challenges and future prospects are provided with a primary focus on single-molecule detection, insufficient sensitivity and stability, lack of validation with large clinical cohorts, and absence of standardization. This review aims to provide researchers with guidance for the rational development of high-performance optical methods to achieve early diagnosis of AD.

Indexed as

Alzheimer DiseaseAmyloid beta-PeptidesBiosensing Techniquestau ProteinsBiomarkersColorimetryHumansSpectrum Analysis, RamanSurface Plasmon ResonanceAmyloid beta-PeptidesBiomarkerstau Proteinsamyloid-betachemiluminescencecolorimetryfluorescencesurface-enhanced Raman scatteringsurface plasmon resonanceTau

Identifiers

PMID42645045
PMCPMC13511098

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.